Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 29 |
NetGPI | no | yes: 0, no: 29 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 30 |
GO:0110165 | cellular anatomical entity | 1 | 30 |
Related structures:
AlphaFold database: E9ATY5
Term | Name | Level | Count |
---|---|---|---|
GO:0038023 | signaling receptor activity | 2 | 3 |
GO:0060089 | molecular transducer activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.373 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.242 |
DOC_CYCLIN_RxL_1 | 293 | 300 | PF00134 | 0.325 |
DOC_MAPK_MEF2A_6 | 161 | 169 | PF00069 | 0.333 |
DOC_PP1_RVXF_1 | 261 | 268 | PF00149 | 0.475 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.451 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.323 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.487 |
LIG_14-3-3_CanoR_1 | 253 | 260 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 4 | 14 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.474 |
LIG_APCC_ABBA_1 | 104 | 109 | PF00400 | 0.415 |
LIG_BRCT_BRCA1_1 | 182 | 186 | PF00533 | 0.242 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.480 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.338 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.428 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.359 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.325 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.305 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.453 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.270 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.537 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.497 |
LIG_IRF3_LxIS_1 | 286 | 291 | PF10401 | 0.333 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 195 | 206 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.183 |
LIG_LIR_Gen_1 | 345 | 355 | PF02991 | 0.319 |
LIG_LIR_LC3C_4 | 210 | 214 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 210 | 214 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 216 | 220 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 241 | 245 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.319 |
LIG_PDZ_Class_2 | 358 | 363 | PF00595 | 0.277 |
LIG_Pex14_1 | 231 | 235 | PF04695 | 0.237 |
LIG_Pex14_1 | 96 | 100 | PF04695 | 0.574 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.301 |
LIG_Pex14_2 | 310 | 314 | PF04695 | 0.303 |
LIG_Pex14_2 | 325 | 329 | PF04695 | 0.415 |
LIG_REV1ctd_RIR_1 | 249 | 257 | PF16727 | 0.301 |
LIG_SH2_CRK | 348 | 352 | PF00017 | 0.219 |
LIG_SH2_NCK_1 | 348 | 352 | PF00017 | 0.219 |
LIG_SH2_STAP1 | 312 | 316 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.204 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.481 |
LIG_TYR_ITIM | 204 | 209 | PF00017 | 0.286 |
LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.313 |
LIG_WRC_WIRS_1 | 186 | 191 | PF05994 | 0.483 |
LIG_WRC_WIRS_1 | 214 | 219 | PF05994 | 0.290 |
LIG_WRC_WIRS_1 | 239 | 244 | PF05994 | 0.375 |
MOD_CDC14_SPxK_1 | 15 | 18 | PF00782 | 0.571 |
MOD_CDK_SPxK_1 | 12 | 18 | PF00069 | 0.574 |
MOD_CDK_SPxxK_3 | 12 | 19 | PF00069 | 0.600 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.698 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.710 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.547 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.404 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.598 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.303 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.279 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.435 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.566 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.503 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.351 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.313 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.663 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.707 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.237 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.510 |
MOD_N-GLC_1 | 39 | 44 | PF02516 | 0.449 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.372 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.227 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.289 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.283 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.277 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.451 |
MOD_OFUCOSY | 221 | 227 | PF10250 | 0.376 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.423 |
MOD_PKA_1 | 4 | 10 | PF00069 | 0.756 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.645 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.339 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.453 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.782 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.603 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.281 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.282 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.264 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.335 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.305 |
MOD_Plk_4 | 99 | 105 | PF00069 | 0.541 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.759 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.392 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.692 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 39 | 47 | PF00179 | 0.551 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.211 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.740 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I280 | Leptomonas seymouri | 64% | 100% |
A0A0N1I909 | Leptomonas seymouri | 34% | 100% |
A0A0N1PEB9 | Leptomonas seymouri | 37% | 67% |
A0A0S4J7T5 | Bodo saltans | 34% | 98% |
A0A0S4J8V2 | Bodo saltans | 42% | 100% |
A0A0S4JQM0 | Bodo saltans | 41% | 100% |
A0A0S4JWI8 | Bodo saltans | 37% | 100% |
A0A0S4KIQ2 | Bodo saltans | 36% | 100% |
A0A1X0P1D6 | Trypanosomatidae | 34% | 100% |
A0A1X0P1Q2 | Trypanosomatidae | 48% | 100% |
A0A3R7L1Y6 | Trypanosoma rangeli | 46% | 100% |
A0A3S7XBT4 | Leishmania donovani | 92% | 100% |
A0A3S7XBU6 | Leishmania donovani | 36% | 71% |
A0A3S7XC05 | Leishmania donovani | 35% | 100% |
A4HQ64 | Leishmania braziliensis | 36% | 71% |
A4HQ67 | Leishmania braziliensis | 79% | 100% |
A4HQ68 | Leishmania braziliensis | 33% | 100% |
A4IDW4 | Leishmania infantum | 92% | 100% |
A4IDW5 | Leishmania infantum | 35% | 71% |
A4IDW6 | Leishmania infantum | 35% | 100% |
B7F9G7 | Oryza sativa subsp. japonica | 29% | 97% |
D0A450 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
D0A451 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ATY6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 73% |
E9ATY7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q03419 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q07959 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 67% |
Q09749 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
Q09910 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 82% |
Q12442 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q4Q0K9 | Leishmania major | 35% | 100% |
Q4Q0L0 | Leishmania major | 35% | 72% |
Q4Q0L1 | Leishmania major | 91% | 100% |
Q6DC77 | Danio rerio | 25% | 100% |
Q6TCG8 | Mus musculus | 30% | 100% |
Q6TCH4 | Homo sapiens | 26% | 100% |
Q6TCH7 | Homo sapiens | 31% | 100% |
Q753H5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 27% | 100% |
Q75F81 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 29% | 87% |
Q801D8 | Cynoscion nebulosus | 26% | 100% |
Q801G2 | Danio rerio | 23% | 100% |
Q84N34 | Arabidopsis thaliana | 30% | 100% |
Q86V24 | Homo sapiens | 33% | 94% |
Q8BQS5 | Mus musculus | 34% | 94% |
Q91VH1 | Mus musculus | 29% | 97% |
Q93ZH9 | Arabidopsis thaliana | 32% | 100% |
Q94177 | Caenorhabditis elegans | 32% | 84% |
Q96A54 | Homo sapiens | 33% | 97% |
Q9DCU0 | Mus musculus | 26% | 100% |
Q9JJE4 | Mus musculus | 28% | 100% |
Q9NXK6 | Homo sapiens | 26% | 100% |
Q9SVF3 | Arabidopsis thaliana | 31% | 97% |
Q9SZG0 | Arabidopsis thaliana | 31% | 94% |
Q9VCY8 | Drosophila melanogaster | 31% | 82% |
Q9ZUH8 | Arabidopsis thaliana | 30% | 100% |
V5BJ57 | Trypanosoma cruzi | 36% | 100% |
V5DK49 | Trypanosoma cruzi | 47% | 100% |